Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
4-Chloro-alpha,alpha,alpha-trifluoro-3-nitrotoluene → 1-Hydroxy-6-(trifluoromethyl)benzotriazole
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | 4-Chloro-alpha,alpha,alpha-trifluoro-3-nitrotoluene | HCID 8462 | — |
| 반응물 | Hydrazine hydrate (1:1) | HCID 24654 | — |
| 용매 | Ethanol | HCID 702 | — |
| 생성물 | 1-Hydroxy-6-(trifluoromethyl)benzotriazole | HCID 688194 | 89.5% |
반응 단계
The title compound is prepared according to the procedure described by K. Takeda [J. Org. Chem., 50, 273, (1985)]. A mixture of 4-chloro-3-nitro-α,α,α-trifluorotoluene (50.0 g, 0.22 moles) and hydrazine hydrate (33.0, 0.33 moles) in absolute ethanol (75 ml) is refluxed for 24 h. After removal of the solvent under reduced pressure, the residue is dissolved in 10% aqueous sodium carbonate solution. The solution is washed with ether to remove the starting material and acidified with concentrated HCl to precipitate the product, which is washed with water and dried to obtain 40.0 g of the title compound. This product is recrystallized from ether.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US07094872B2 |
| 출처 데이터셋 | uspto-grants-2006_08 |
| ORD ID | ord-868789ba44d24a379570d31b85128dc2 |
| 출처 메모 | uspto-grants-2006_08 |